NDC 66343-039 Emvita 27

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
66343-039
Proprietary Name:
Emvita 27
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Rubimed Ag
Labeler Code:
66343
Start Marketing Date: [9]
05-07-2015
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 66343-039-50

Package Description: 50 mL in 1 BOTTLE, DROPPER

Product Details

What is NDC 66343-039?

The NDC code 66343-039 is assigned by the FDA to the product Emvita 27 which is product labeled by Rubimed Ag. The product's dosage form is . The product is distributed in a single package with assigned NDC code 66343-039-50 50 ml in 1 bottle, dropper . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Emvita 27?

This product is used as Homeopathic Combination Medicine Indications: Inability to face reality

Which are Emvita 27 UNII Codes?

The UNII codes for the active ingredients in this product are:

  • HELLEBORUS NIGER ROOT (UNII: 608DGJ6815)
  • HELLEBORUS NIGER ROOT (UNII: 608DGJ6815) (Active Moiety)
  • MANDRAGORA OFFICINARUM ROOT (UNII: I2XCB174VB)
  • MANDRAGORA OFFICINARUM ROOT (UNII: I2XCB174VB) (Active Moiety)
  • ANACARDIUM OCCIDENTALE FRUIT (UNII: 4A10JR4E7E)
  • ANACARDIUM OCCIDENTALE FRUIT (UNII: 4A10JR4E7E) (Active Moiety)
  • LOPHOPHORA WILLIAMSII FLOWER (UNII: N7FOQ6M7DZ)
  • LOPHOPHORA WILLIAMSII FLOWER (UNII: N7FOQ6M7DZ) (Active Moiety)
  • SUS SCROFA CEREBELLUM (UNII: 49NGK53TPQ)
  • SUS SCROFA CEREBELLUM (UNII: 49NGK53TPQ) (Active Moiety)

Which are Emvita 27 Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

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Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".